| Literature DB >> 31030757 |
Pengjiao Zeng1, Juan Li2, Yulong Chen3, Lijuan Zhang4.
Abstract
Most of traditional Chinese medicine substances come from herbal plants. The medicinal quality of herbal plants varies with the locations of cultivation, the parts of the herb collected, the season of the herb collected, and the herb processing method. Polysaccharides are major components of the herb plants and their biosynthesis is partly controlled by the genes but mostly influenced by the availability of the nutrition and determined by the various environmental factors. In recent decades, polysaccharides isolated from different kinds of Chinese herbs have received much attention due to their important biological activities, such as anti-tumor, anti-oxidant, anti-diabetic, radiation protecting, antiviral, hypolipidemic, and immunomodulatory activities. Interestingly, different batches of the same herb can obtain different polysaccharide fractions with subtle differences in molecular weight, monosaccharide compositions, glycosidic linkages, and biological functions. Even with these variations, a large number of bioactive polysaccharides from different kinds of traditional Chinese herbs have been purified, characterized, and reported. This review provides a comprehensive summary of the latest polysaccharide extraction methods and the strategies used for monosaccharide compositional analysis plus polysaccharide structural characterization. Most importantly, the reported chemical characteristics and biological activities of the polysaccharides from the famous traditional Chinese herbs including Astragalus membranaceus, Ginseng, Lycium barbarum, Angelica sinensis, Cordyceps sinensis, and Ophiopogon japonicus will be reviewed and discussed. The published studies provide evidence that polysaccharides from traditional Chinese herbs play an important role in their medical applications, which forms the basis for future research, development, and application of these polysaccharides as functional foods and therapeutics in modern medicine.Entities:
Keywords: Biological activity; Chemical structure; Extraction method; Polysaccharides; Traditional Chinese herbs
Mesh:
Substances:
Year: 2019 PMID: 31030757 PMCID: PMC7102684 DOI: 10.1016/bs.pmbts.2019.03.003
Source DB: PubMed Journal: Prog Mol Biol Transl Sci ISSN: 1877-1173 Impact factor: 3.622
Polysaccharide extraction, separation and purification methods from traditional Chinese herbs.
| Contents | Methods | Features | ||
|---|---|---|---|---|
| Extraction | Acid–base or water | Prevent glycosidic bond break | ||
| Enzymatic | Mild conditions, lower damage, higher yield, avoiding changes in physiological activity | |||
| Microwave-assisted | High yield, shorter extraction time and lower cost | |||
| Ultrasound-assisted | Faster, energy-saving, higher yield | |||
| Ultra high pressure | Shorter time and high efficiency | |||
| Isolation and purification | Miscellaneous | Removing proteins | Sevage method | Troublesome, time-consuming, large amount of reagents, structural damage, and large losses |
| Trichloroacetic acid | Effect but destroying structure | |||
| Protease | Mild and efficient | |||
| Decolorization | Activated carbon adsorption | Stronger affinity adsorption, larger loss | ||
| Hydrogen peroxide | Pigment containing unsaturated double bonds, hydroxyl groups and aromatic rings | |||
| Ion exchange | High decolorization and retention rate | |||
| Small molecule impurities | Dialysis | – | ||
| Fractional purification | Precipitation | Polysaccharides with differences in solubility | ||
| Gel chromatography | – | |||
| Anion exchange chromatography | Crude purification of polysaccharide | |||
| Macroporous resin column chromatography | Have no effect on the biological activity | |||
| Ultrafiltration | High separation efficiency, low energy consumption, no pollution and no damage to polysaccharide activity, easy to be contaminated | |||
Summary of structural and biological activities of polysaccharides from six traditional Chinese herbs.
| Species | Glycans | Extraction methods | Major monosaccharides | Glycosidic linkage in backbone | MW (Da) | Bioactivities | References |
|---|---|---|---|---|---|---|---|
| Hot water,ultrasonic and microwave extraction, DEAE-Sephadex A-25, Sephadex G-100 | Rhamnose, arabinose, xylose, ribose, galactose, glucose, mannose, fructose, fucose | α-(1 → 4)-Glc; α(1 → 3)-Gal | 8.7–4800 K | Immunomodulation | |||
| Anti-inflammation | |||||||
| Anti-oxidant | |||||||
| Anti-glomerulonephritis | |||||||
| Anti-atherosclerosis | |||||||
| Anti-diabetes | |||||||
| Anti-tumor | 49 | ||||||
| Hot water, ethanol fractionation, DEAE-Sepharose-CL-6B, Sepharose-CL-6B, Sephadex-G-75 | α-(1 → 3)-Ara; β-(1 → 3) or β-(1 → 4) Gal | 3.2–1900 K | Antibacterial | ||||
| Anti-oxidant | |||||||
| Anti-inflammatory | |||||||
| Anti-depressant | |||||||
| Anti-tumor | |||||||
| Immunomodulation | |||||||
| Warm water extraction, DEAE cellulose column, Sephadex G-150 | Glucose, arabinose, galactose, mannose, xylose, rhamnose, fucose, galacturonic acid, glucuronic acid | β-(1 → 3) or β-(1 → 4) Gal; α-(1 → 6)-Glc | Average 49.1 K | Anti-oxidant | |||
| Anti-tumor | |||||||
| Anti-radiation | |||||||
| Anti-fatigue | |||||||
| Anti-aging | |||||||
| Anti-inflammation | |||||||
| Immunomodulation | |||||||
| Water extraction, SephadexG-100, DEAE-52 | Glucose, mannose, galactose, rhamnose, arabinose, xylose | α(1,4)-Glc | 5.1–2300 K | Immunomodulation | |||
| Anti-tumor | |||||||
| Hepatoprotective | |||||||
| Anti-diabetic | |||||||
| Gastrointestinal protection | |||||||
| Hot water extraction, DEAE-Sepharose Fast Flow, Sephadex G-75 | Mannose, glucose, galactose, galacturonic acid | α(1 → 2) or α(1 → 4)-Man-α(1 → 4)-Glc | 7.7–210 K | Immunomodulation | |||
| Anti-tumor | |||||||
| Anti-oxidant | |||||||
| Anti-diabetes | |||||||
| Anti-aging | |||||||
| Anti-scald | |||||||
| Hot water, ultrasonic and enzymatic water extraction, DEAE-52,Sephadex G-100 | Fructose, glucose, arabinose, mannose | Fru-β (2 →,→2)-Fru-β(6 →,→6)-Glc-α(1 → and → 1.2)-Fru-β (6 →) | 3.4–48.7 K | Anti-myocardial infarction | |||
| Anti-diabetes | |||||||
| Anti-oxidant | |||||||
| Immunomodulation | |||||||
| Anti-thrombotic |
Fig. 1Immune regulatory mechanisms of herb polysaccharides.
Analytical methods for identifying monosaccharide compositions, molecular weight distributions, and glycosidic linkages of polysaccharides.
| Items | Methods |
|---|---|
| Determination of purity and relative molecular weight distributions of polysaccharides | HPGPC, osmotic pressure, viscosity method, light scattering method, polyacrylamide gel electrophoresis |
| Monosaccharide compositional analysis | Complete acid hydrolysis, HPLC, GC, GC–MS, ion chromatography |
| Glycoside ring form (pyran, furan) | Infrared spectrum |
| Glycosidic linkages of the polysaccharide | Methylation analysis, GC–MS, LC–MS |
| The anomeric forms substituted by glycosides (α- and β-) | Glycosidase hydrolysis, nuclear magnetic resonance, infrared spectroscopy, laser Raman spectroscopy, etc. |
| Sequence of the oligosaccharides | Elective acid hydrolysis, sequential hydrolysis by glycosidases, nuclear magnetic resonance, etc. |
| The hydroxyl positions in the monosaccharide | Methylation, periodate oxidation, Smith degradation, GC–MS, nuclear magnetic resonance, etc. |
| Polysaccharide-peptide linkage | Dilute alkali hydrolysis method, hydrazine reaction, amino acid composition analysis, etc. |